Symptoms of neuroblastoma recurrence

Written by Chen Yu Fei
Neurosurgery
Updated on November 08, 2024
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For neuroblastoma, when the tumor recurs, the patient's original symptoms such as headaches, dizziness, nausea, and vomiting will reappear, occurring intermittently and worsening persistently. Most patients will experience significant increased intracranial pressure, and even frequent nausea and vomiting. Additionally, some neuroblastoma patients experience severe vertigo, especially when changing body positions, where the vertigo is particularly pronounced. For such patients, when the above symptoms and signs occur, they should go to a local hospital as soon as possible for a reassessment using cranial MRI to monitor changes in their condition.

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Neuroblastoma in children

Neuroblastoma does not specifically concern how old the child is, as it can occur in children during their developmental process, and even in newborns, adolescents, and adults. There is no specific timing required for its occurrence. Therefore, for neuroblastoma, the principle is to initiate treatment as soon as it is detected. Although the prognosis may not be very good, the aim should be to extend the patient's life and reduce suffering as much as possible. After all, no matter the age, the patient is a loved one.

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Is neuroblastoma serious?

Neuroblastoma is relatively serious and is classified as a highly malignant tumor, one of the epithelial cell tumors. The disease often leads to severe intracranial pressure increases, manifesting as intense headaches, dizziness, nausea, vomiting, and even possible optic disc edema, vision loss, and visual field defects. The occurrence of neuroblastoma often indicates a poor prognosis for patients, with a short disease duration and reduced survival time. The five-year survival rate is decreased. Treatment primarily involves surgical intervention to completely remove the neuroblastoma, followed by postoperative radiotherapy, chemotherapy, and other related treatments.

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Written by Chen Yu Fei
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How do you get neuroblastoma?

Currently, there is no consensus on the specific causes of neuroblastoma. In most cases, it is believed to be caused by the failure of primitive myeloid epithelial cells to continue differentiating, which is somewhat linked to congenital genetic factors. Additionally, poor lifestyle choices and exposure to certain chemical carcinogens, including long-term exposure to radiation, can potentially lead to neuroblastoma. Neuroblastoma is a highly malignant tumor that generally grows and develops rapidly. It often adheres to surrounding tissues in the early stages of the disease, making complete surgical removal quite difficult, and typically has a poor prognosis.

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How is neuroblastoma diagnosed?

For patients with neuroblastoma, diagnosis is primarily through the symptoms, signs, detailed physical examinations, medical history inquiries, and most importantly, radiological data, which includes CT scans or MRI of the head. Definitive diagnosis requires surgical removal of the tumor. A small amount of tumor tissue is retained after excision and used for pathological examination to confirm the diagnosis. Neuroblastoma is categorized as an epithelial-like malignant tumor, indicative of a high degree of malignancy. In most cases, early in the disease, the tumor adheres to surrounding tissues, which greatly complicates complete surgical removal, and most patients have a poor prognosis.

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Is neuroblastoma a cancer?

Neuroblastoma is a highly malignant tumor, one of the most malignant among neuroepithelial tumors, and thus can be considered as cancer from this perspective. Typically, its tumor biology growth pattern is that of a malignant tumor, often growing rapidly. In the early stages of the disease, it tends to adhere closely to surrounding tissues, making it difficult for surgery to be completely successful. In addition, during treatment, it can be observed that the tumor cells are highly invasive to surrounding tissues. This often leads to significant brain edema, resulting in compression of important surrounding blood vessels and nerves, causing functional damage. The tumor can also spread through the bloodstream, making it difficult to completely remove surgically, or to miss the optimal time for surgical treatment, resulting in a poor prognosis.